Two series of 2,4,6-tris(amino)-s-triazines were studied by 1 H and 13 C NMR. 15 N NMR had previously demonstrated hindered rotation of the acyclic amino substituents (NHallyl, NHpropyl) around the Ar -N bonds at room temperature. In the present work, 1 H and 13 C NMR studies showed that rotation is
Micellar Solubilization: Structural and Conformational Changes Investigated by 1H and 13C Liquid-State NMR
✍ Scribed by Bruno Alonso; Robin K. Harris; Alan M. Kenwright
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 233 KB
- Volume
- 251
- Category
- Article
- ISSN
- 0021-9797
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